Subscribe to RSS
DOI: 10.1055/a-0725-8456
Rosehip Oil Promotes Excisional Wound Healing by Accelerating the Phenotypic Transition of Macrophages
Publication History
received 03 June 2018
revised 18 August 2018
accepted 24 August 2018
Publication Date:
10 September 2018 (online)
Abstract
Poor wound healing is a major and global threat to public health. Efforts have been made to better understand the underlying mechanisms and develop effective remedies, though the advancements that have been made are still limited. As there are no effective and generally applicable therapies available for skin injuries and fibrosis, it is urgent to develop new drugs and therapies that facilitate wound healing and effectively improve scars. In this study, GC-MS analysis was performed to identify the chemical composition of rosehip oil. The excisional wound healing model and the carrageenan-induced paw edema method were respectively applied to evaluate the wound healing activity and anti-inflammatory activity of rosehip oil. Hematoxylin and eosin staining was used to assess the pathological changes of sections, and Sirius-red staining was performed to analyze the ratio of collagen I/III in wound tissues. Immunohistological staining for CD68, CCR7 (CD197), CD163, TGF-β1, and α-SMA was applied to determine the macrophage phenotypes transition (M1-to-M2) and demonstrate the scar-improving efficacy of rosehip oil on wound healing. Results showed that rosehip oil significantly promoted wound healing and effectively improved scars. This efficacy might be exerted by accelerating the macrophage phenotypes transition and inhibiting the process of epithelial-mesenchymal transition.
Key words
wound healing - excisional wound - anti-inflammatory activity - rosehip oil - Rosa canina - RosaceaeSupporting Information
- Supporting Information
A GC-MS chromatogram of RO and pictures of wounds taken on days 0, 2, 5, 7, 10, 14, and 21 are available as Supporting Information.
-
References
- 1 Robson MC, Steed DL, Franz MG. Wound healing: biologic features and approaches to maximize healing trajectories. Curr Probl Surg 2001; 38: 72-140
- 2 Weiser TG, Regenbogen SE, Thompson KD, Haynes AB, Lipsitz SR, Berry WR, Gawande AA. An estimation of the global volume of surgery: a modelling strategy based on available data. Lancet 2008; 372: 139-144
- 3 Erickson JR, Echeverri K. Learning from regeneration research organisms: The circuitous road to scar free wound healing. Dev Biol 2018; 433: 144-154
- 4 Vision Gain. Advanced wound care: world market prospects 2011–2021. Available at: http://www.visiongain.com/Report/716/Advanced-Wound-Care-World-Market-Prospects-2011-2021 Accessed November 15, 2011
- 5 Sen CK, Gordillo GM, Roy S, Kirsner R, Lambert L, Hunt TK, Gottrup F, Gurtner GC, Longaker MT. Human skin wounds: a major and snowballing threat to public health and the economy. Wound Rep Reg 2009; 17: 763-771
- 6 Mukherjee H, Ojha D, Bharitkar YP, Ghosh S, Mondal S, Kaity S, Dutta S, Samanta A, Chatterjee TK, Chakrabarti S, Mondal NB, Chattopadhyay D. Evaluation of the wound healing activity of Shorea robusta, an Indian ethnomedicine, and its isolated constituent(s) in topical formulation. J Ethnopharmacol 2013; 149: 335-343
- 7 Kasuya A, Tokura Y. Attempts to accelerate wound healing. J Dermatol Sci 2014; 76: 169-172
- 8 Zomer HD, Trentin AG. Skin wound healing in humans and mice: Challenges in translational research. J Dermatol Sci 2018; 90: 3-12
- 9 Miller MC, Nanchahal J. Advances in the modulation of cutaneous wound healing and scarring. BioDrugs 2005; 19: 363-381
- 10 Behm B, Babilas P, Landthaler M, Schreml S. Cytokines, chemokines and growth factors in wound healing. J Eur Acad Dermatol 2012; 26: 812-820
- 11 Bielefeld KA, Amini-Nik S, Alman BA. Cutaneous wound healing: recruiting developmental pathways for regeneration. Cell Mol Life Sci 2013; 70: 2059-2081
- 12 Guo S, DiPietro LA. Factors affecting wound healing. J Dent Res 2010; 89: 219-229
- 13 Udupa AL, Kulkarni DR, Udupa SL. Effect of Tridax procumbens extracts on wound healing. Int J Pharmacogn 1995; 33: 37-40
- 14 Perez JL, Rohrich RJ. Optimizing postsurgical scars: a systematic review on best practices in preventative scar management. Plast Reconstr Surg 2017; 140: 782e-793e
- 15 Das U, Behera SS, Pramanik K. Ethno-herbal-medico in wound repair: an incisive review. Phytother Res 2017; 31: 579-590
- 16 Wedler J, Daubitz T, Schlotterbeck G, Butterweck V. In vitro anti-inflammatory and wound-healing potential of a Phyllostachys edulis leaf extract-identification of isoorientin as an active compound. Planta Med 2014; 80: 1678-1684
- 17 Gautam MK, Gangwar M, Singh SK, Goel RK. Effects of Azardirachta indica on vascular endothelial growth factor and cytokines in diabetic deep wound. Planta Med 2015; 81: 713-721
- 18 Verjee S, Garo E, Pelaez S, Fertig O, Hamburger M, Butterweck V. Saffron flower extract promotes scratch wound closure of keratinocytes and enhances VEGF production. Planta Med 2017; 83: 1176-1183
- 19 Ilyasoğlu H. Characterization of rosehip (Rosa canina L.) seed and seed oil. Int J Food Prop 2014; 17: 1591-1598
- 20 Osojnik Črnivec IG, Muri P, Djinović P, Pintar A. Biogas production from spent rose hips (Rosa canina L.): fraction separation, organic loading and co-digestion with N-rich microbial biomass. Bioresour Technol 2014; 171: 375-383
- 21 Paladines D, Valero D, Valverde JM, Díaz-Mula H, Serrano M, Martínez-Romero D. The addition of rosehip oil improves the beneficial effect of Aloe vera gel on delaying ripening and maintaining postharvest quality of several stonefruit. Postharvest Biol Tec 2014; 92: 23-28
- 22 Zhao G, Etherton TD, Martin KR, Vanden Heuvel JP, Gillies PJ, West SG, Kris-Etherton PM. Anti-inflammatory effects of polyunsaturated fatty acids in THP-1 cells. Biochem Biophys Res Commun 2005; 336: 909-917
- 23 Delmastro-Greenwood M, Freeman BA, Wendell SG. Redox-dependent anti-inflammatory signaling actions of unsaturated fatty acids. Annu Rev Physiol 2014; 76: 79-105
- 24 Nissinen LM, Kahari VM. Collagen turnover in wound repair – a macrophage connection. J Invest Dermatol 2015; 135: 2350-2352
- 25 Zhu Z, Ding J, Tredget EE. The molecular basis of hypertrophic scars. Burns Trauma 2016; 4: 2
- 26 Moore KW, de Waal MR, Coffman RL, OʼGarra A. Interleukin-10 and the interleukin-10 receptor. Annu Rev Immunol 2001; 19: 683-765
- 27 Sindrilaru A, Peters T, Wieschalka S, Baican C, Baican A, Peter H, Hainzl A, Schatz S, Qi Y, Schlecht A, Weiss JM, Wlaschek M, Sunderkötter C, Scharffetter-Kochanek K. An unrestrained proinflammatory M1 macrophage population induced by iron impairs wound healing in humans and mice. J Clin Invest 2011; 121: 985-997
- 28 Mirza RE, Fang MM, Novak ML, Urao N, Sui A, Ennis WJ, Koh TJ. Macrophage PPARγ and impaired wound healing in type 2 diabetes. J Pathol 2015; 236: 433-444
- 29 Khanna S, Biswas S, Shang Y, Collard E, Azad A, Kauh C, Bhasker V, Gordillo GM, Sen CK, Roy S. Macrophage dysfunction impairs resolution of inflammation in the wounds of diabetic mice. PLoS One 2010; 5: e9539
- 30 Mueller CK, Schultze-Mosgau S. Histomorphometric analysis of the phenotypical differentiation of recruited macrophages following subcutaneous implantation of an allogenous acellular dermal matrix. Int J Oral Max Surg 2011; 40: 401-407
- 31 Manduch M, Dexter DF, Jalink DW, Vanner SJ, Hurlbut DJ. Undifferentiated pancreatic carcinoma with osteoclast-like giant cells: report of a case with osteochondroid differentiation. Pathol Res Pract 2009; 205: 353-359
- 32 Hopken UE, Winter S, Achtman AH, Kruger K, Lipp M. CCR7 regulates lymphocyte egress and recirculation through body cavities. J Leukoc Biol 2010; 87: 671-682
- 33 Siebert JW, Burd AR, McCarthy JG, Weinzweig J, Ehrlich HP. Fetal wound healing: a biochemical study of scarless healing. Plast Reconstr Surg 1990; 85: 495-502
- 34 Merkel JR, DiPaolo BR, Hallock GG, Rice DC. Type I and type III collagen content of healing wounds in fetal and adult rats. Exp Biol Med 1988; 187: 493-497
- 35 Hallock GG, Ricem DC, Merkel JR, DiPaolo BR. Analysis of collagen content in the fetal wound. Ann Plast Surg 1988; 21: 310-315
- 36 Cameron AM, Adams DH, Greenwood JE, Anderson PJ, Cowin AJ. A novel murine model of hypertrophic scarring using subcutaneous infusion of bleomycin. Plast Reconstr Surg 2014; 133: 69-78
- 37 Tomasek JJ, Gabbiani G, Hinz B, Chaponnier C, Brown RA. Myofibroblasts and mechano-regulation of connective tissue remodelling. Nat Rev Mol Cell Bio 2002; 3: 349-363
- 38 Van De Water L, Varney S, Tomasek JJ. Mechanoregulation of the myofibroblast in wound contraction, scarring, and fibrosis: opportunities for new therapeutic intervention. Adv Wound Care 2013; 2: 122-141
- 39 Pohlers D, Brenmoehl J, Löffler I, Müller CK, Leipner C, Schultze-Mosgau S, Stallmach A, Kinne RW, Wolf G. TGF-β and fibrosis in different organs – molecular pathway imprints. Biochim Biophys Acta 2009; 1792: 746-756
- 40 FDA. 2006 Guidance for industry: chronic cutaneous ulcer and burn wounds-developing products for treatment. Official publication of the US Department of Health and Human Services – Food and Drug Administration (FDA) – Center for Drug Evaluation and Research (CDER) – Center for Biologics Evaluation and Research (CBER) – Center for Devices and Radiological Health (CDRH) pp. 18. Available at at: http://www.fda.gov/cber/gdlns/ulcburn.htm Accessed June 1, 2006
- 41 Mu Y, Xu Z, Zhou X, Zhang H, Yang Q, Zhang Y, Xie Y, Kang J, Li F, Wang S. 2,3,5,4-Tetrahydroxystilbene-2-O-β-D-glucoside attenuates ischemia/reperfusion-induced brain injury in rats by promoting angiogenesis. Planta Med 2017; 83: 676-683